Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K150052 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring d... | 1 | 03/12/2026 |
FEI # 1000113657 Trividia Health, Inc. |
| TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative m... | 2 | 06/01/2020 |
FEI # 1000113657 Trividia Health, Inc. |
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